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圆形轨迹重建从单细胞Hi-C图谱中揭示细胞周期进程和调控动态

Circular Trajectory Reconstruction Uncovers Cell-Cycle Progression and Regulatory Dynamics from Single-Cell Hi-C Maps.

作者信息

Ye Yusen, Gao Lin, Zhang Shihua

机构信息

School of Computer Science and Technology Xidian University Xi'an 710071 Shaanxi China.

NCMIS CEMS RCSDS Academy of Mathematics and Systems Science Chinese Academy of Sciences Beijing 100190 China.

出版信息

Adv Sci (Weinh). 2019 Sep 30;6(23):1900986. doi: 10.1002/advs.201900986. eCollection 2019 Dec.

Abstract

Single-cell Hi-C technology is emerging and will provide unprecedented opportunities to elucidate chromosomal dynamics with high resolution. How to characterize pseudo time-series of single cells using single-cell Hi-C maps is an essential and challenging topic. To this end, a powerful circular trajectory reconstruction tool CIRCLET is developed to resolve cell cycle phases of single cells by considering multiscale features of chromosomal architectures without specifying a starting cell. CIRCLET reveals its best superiority based on the combination of one feature set about global information and another two feature sets about local interactional information in terms of designed evaluation indexes and verification strategies from a collection of cell-cycle Hi-C maps of 1171 single cells. Further division of the reconstructed trajectory into 12 stages helps to accurately characterize the dynamics of chromosomal structures and explain the special regulatory events along cell-cycle progression. Last but not the least, the reconstructed trajectory helps to uncover important regulatory genes related with dynamic substructures, providing a novel framework for discovering regulatory regions even cancer markers at single-cell resolution.

摘要

单细胞Hi-C技术正在兴起,将为高分辨率阐明染色体动力学提供前所未有的机会。如何利用单细胞Hi-C图谱表征单细胞的伪时间序列是一个重要且具有挑战性的课题。为此,开发了一种强大的圆形轨迹重建工具CIRCLET,通过考虑染色体结构的多尺度特征来解析单细胞的细胞周期阶段,而无需指定起始细胞。基于1171个单细胞的细胞周期Hi-C图谱集合所设计的评估指标和验证策略,CIRCLET在一个关于全局信息的特征集与另外两个关于局部相互作用信息的特征集相结合的基础上展现出其最佳优势。将重建的轨迹进一步划分为12个阶段有助于准确表征染色体结构的动态变化,并解释细胞周期进程中的特殊调控事件。最后但同样重要的是,重建的轨迹有助于发现与动态子结构相关的重要调控基因,为在单细胞分辨率下发现调控区域甚至癌症标志物提供了一个新的框架。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc3a/6891923/c305fe97c2af/ADVS-6-1900986-g001.jpg

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